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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-2171-2017
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1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Systems (Part Number M8275093/5). ... 2 05/30/2017 FEI # 3009897021
KCI USA, INC.
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